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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383637Generated: October 31, 2026

4-Methylmorpholine → Ethyl[3-(3-{4-[(2-acetylaminoacetylamino)methyl]phenyl}-6-oxo-6h-pyridazin-1-ylmethyl)phenyl]carbamate

https://huagongshe.com/reaction/383637

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantAcetylglycineHCID 10972—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantEthyl{3-[3-(4-aminomethylphenyl)-6-oxo-6h-pyridazin-1-ylmethyl]phenyl}carbamateHCID 59406699—
SolventDimethylformamideHCID 6228—
ProductEthyl[3-(3-{4-[(2-acetylaminoacetylamino)methyl]phenyl}-6-oxo-6h-pyridazin-1-ylmethyl)phenyl]carbamateHCID 25118490—

Reaction Steps

61 mg (0.52 mmol) of N-acetylglycine are suspended in 2 ml of DMF, 106 μl (0.95 mmol) of 4-methylmorpholine, 66 mg (0.47 mmol) of 1-hydroxybenzotriazole and 184 mg (0.95 mmol) of N-(3-dimethylamino-propyl)-N′-ethylcarbodiimide hydrochloride are added. The reaction mixture is stirred at room temperature for 10 min, 180 mg (0.48 mmol) of ethyl{3-[3-(4-aminomethylphenyl)-6-oxo-6H-pyridazin-1-ylmethyl]-phenyl}carbamate are subsequently added, and the mixture is stirred at room temperature for 24 h.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367668B2
Source datasetuspto-grants-2013_02
ORD IDord-956ff54e833c41dd962f219daf89fbf4
Source noteuspto-grants-2013_02